Fine-mapping of Naegeli-Franceschetti-Jadassohn syndrome to 7 cM in 17q11.2-q21, and exclusion of 18 positional candidate genes.

被引:0
|
作者
Sprecher, E
Itin, P
Whittock, N
McGrath, J
Uitto, J
Richard, G
机构
[1] Rambam Med Ctr, Haifa, Israel
[2] Thomas Jefferson Univ, Philadelphia, PA 19107 USA
[3] Univ Basel, CH-4003 Basel, Switzerland
[4] St Johns Inst Dermatol, London, England
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
2155
引用
收藏
页码:384 / 384
页数:1
相关论文
共 13 条
  • [1] Refined mapping of Naegeli-Franceschetti-Jadassohn syndrome to a 6 cM interval on chromosome 17q11.2-q21 and investigation of candidate genes
    Sprecher, E
    Itin, P
    Whittock, NV
    McGrath, JA
    Meyer, R
    DiGiovanna, JJ
    Bale, SJ
    Uitto, J
    Richard, G
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2002, 119 (03) : 692 - 698
  • [2] The gene for Naegeli-Franceschetti-Jadassohn syndrome maps to 17q21
    Whittock, NV
    Coleman, CM
    McLean, WH
    Ashton, GHS
    Acland, KM
    Eady, RAJ
    McGrath, JA
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2000, 115 (04) : 694 - 698
  • [3] Infantile autism - Fine mapping of a candidate region on chromosome 7q and association studies of candidate genes.
    Klauck, SM
    Beyer, KS
    Benner, A
    Poustka, F
    Poustka, A
    AMERICAN JOURNAL OF MEDICAL GENETICS, 2000, 96 (04): : 479 - 479
  • [4] Fine-Mapping of Genomic Regions on Chromosomes 5q, 7q, 21p and 22q Identifies Candidate Genes for Proteinuria in Type 2 Diabetes
    Pezzolesi, Marcus G.
    Skupien, Jan
    Poznik, G. David
    Smiles, Adam
    Mychaleckyj, Josyf C.
    Rich, Stephen S.
    Warram, James H.
    Krolewski, Andrzej S.
    DIABETES, 2010, 59 : A110 - A110
  • [5] Fine-mapping the 2q37 and 17q11.2-q22 loci for novel genes and sequence variants associated with a genetic predisposition to prostate cancer
    Laitinen, Virpi H.
    Rantapero, Tommi
    Fischer, Daniel
    Vuorinen, Elisa M.
    Tammela, Teuvo L. J.
    Wahlfors, Tiina
    Schleutker, Johanna
    INTERNATIONAL JOURNAL OF CANCER, 2015, 136 (10) : 2316 - 2327
  • [6] Search for genetic variants in positional candidate genes on chromosome 7q21 for association with metabolic syndrome in Mexican Americans
    Farook, Vidya S.
    Puppala, Sobha
    Arya, Rector
    Schneider, Jennifer
    Fowler, Sharon
    Dyer, Thomas D.
    Cole, Shelly A.
    Almasy, Laura
    Blangero, John
    Stern, Michael P.
    Duggirala, Ravindranath
    DIABETES, 2006, 55 : A256 - A256
  • [7] Fine-mapping the putative chromosome 17q21-22 prostate cancer susceptibility gene to a 10 cM region based on linkage analysis
    Lange, Ethan M.
    Robbins, Christiane M.
    Gillanders, Elizabeth M.
    Zheng, Siqun Lilly
    Xu, Jianfeng
    Wang, Yunfei
    White, Kirsten A.
    Chang, Bao-Li
    Ho, Lindsey A.
    Trent, Jeffrey M.
    Carpten, John D.
    Isaacs, William B.
    Cooney, Kathleen A.
    HUMAN GENETICS, 2007, 121 (01) : 49 - 55
  • [8] Fine-mapping the putative chromosome 17q21–22 prostate cancer susceptibility gene to a 10 cM region based on linkage analysis
    Ethan M. Lange
    Christiane M. Robbins
    Elizabeth M. Gillanders
    Siqun Lilly Zheng
    Jianfeng Xu
    Yunfei Wang
    Kirsten A. White
    Bao-Li Chang
    Lindsey A. Ho
    Jeffrey M. Trent
    John D. Carpten
    William B. Isaacs
    Kathleen A. Cooney
    Human Genetics, 2007, 121 : 49 - 55
  • [9] Search for genetic variants in positional candidate genes on chromosome 7q21 region linked to metabolic syndrome in Mexican Americans
    Farook, Vidya S.
    Puppala, Sobha
    Arya, Rector
    Schneider, Jennifer
    Fowler, Sharon P.
    Dyer, Thomas D.
    Cole, Shelly A.
    Almasy, Laura
    Blangero, John
    Duggirala, Ravindranath
    DIABETES, 2007, 56 : A305 - A305
  • [10] GENETIC-MAPPING OF THE BREAST-OVARIAN CANCER SYNDROME TO A SMALL INTERVAL ON CHROMOSOME-17Q12-21 - EXCLUSION OF CANDIDATE GENES EDH17B2 AND RARA
    SIMARD, J
    FEUNTEUN, J
    LENOIR, G
    TONIN, P
    NORMAND, T
    THE, VL
    VIVIER, A
    LASKO, D
    MORGAN, K
    ROULEAU, GA
    LYNCH, H
    LABRIE, F
    NAROD, SA
    HUMAN MOLECULAR GENETICS, 1993, 2 (08) : 1193 - 1199